pravastatin sodium
- Product NDC
- 63629-4588
- 11-digit product format
- 636294588
- Labeler code
- 63629
- Product ID
- 63629-4588_de916393-2e70-492c-9fe4-1158187efe9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077751
- Marketing category
- ANDA
- Marketing start
- 2010-03-30
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4588-1 | 63629458801 | 30 TABLET in 1 BOTTLE (63629-4588-1) | 30 tablet | 2011-09-06 | 0000-00-00 | No | No | Current |
| 63629-4588-2 | 63629458802 | 90 TABLET in 1 BOTTLE (63629-4588-2) | 90 tablet | 2012-03-28 | 0000-00-00 | No | No | Current |
| 63629-4588-3 | 63629458803 | 10 TABLET in 1 BOTTLE (63629-4588-3) | 10 tablet | 2022-02-08 | 0000-00-00 | No | No | Current |